Charlotte S. Goutallier MD , Alayna Carrandi MPH , Shaun P. Brennecke MBBS, DPhil , Emily J. Callander PhD
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The objective of this systematic review is to determine the cost-effectiveness of the sFlt-1/PlGF ratio test globally for pregnant patients at-risk of developing PE.</div></div><div><h3>Data sources</h3><div>PubMed, Medline (OVID), National Health Service Economic Evaluation Database, Web of Science, Econlit, and Cost Effectiveness Analysis Registry was systematically searched between 2013-April 2023.</div></div><div><h3>Study eligibility criteria</h3><div>Empirical studies quantifying costs of the sFlt-1/PlGF ratio test compared to other diagnostic options for pregnant patients with suspected PE.</div></div><div><h3>Study appraisal and synthesis methods</h3><div>Eleven studies were included in the systematic review; all were cost analyses and modelled economic evaluations, and most used a health system perspective. Cost data were extracted into tables and indexed to 2022 United States Dollars (USD). An assessment of risk of bias for each study was performed using the Drummond critical appraisal checklist.</div></div><div><h3>Results</h3><div>All studies reported “cost-savings” of the test in antenatal care. Studies varied with costs and assumptions included, therefore a large range of incremental cost savings per patient was reported ($15–$1,881, 2022USD). No Incremental Cost-Effectiveness Ratios or health outcomes including Quality Adjusted Life Years were reported.</div></div><div><h3>Conclusions</h3><div>The included studies demonstrated “cost-savings” of the sFlt-1/PlGF ratio test in antenatal care for at-risk pregnant patients. However, this does not account for health outcome differences and long-term health care utilisation and expenditure.</div></div>","PeriodicalId":72141,"journal":{"name":"AJOG global reports","volume":"5 2","pages":"Article 100498"},"PeriodicalIF":0.0000,"publicationDate":"2025-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Cost-effectiveness of the sFlt-1/PlGF ratio test in pregnant patients with suspected pre-eclampsia: a systematic review\",\"authors\":\"Charlotte S. Goutallier MD , Alayna Carrandi MPH , Shaun P. Brennecke MBBS, DPhil , Emily J. Callander PhD\",\"doi\":\"10.1016/j.xagr.2025.100498\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Objectives</h3><div>Pre-eclampsia (PE) affects approximately 2%–4% of pregnancies. Diagnosis involves repeated assessment of pregnant patients with risk factors. The sFlt-1/PlGF ratio test is shown to have clinical utility in ruling in and out PE among at-risk patients. By excluding the probability of PE, the addition of the sFlt-1/PlGF ratio test to antenatal care may prevent unnecessary hospital admissions, intensive management, and premature delivery, thus reducing costs. The objective of this systematic review is to determine the cost-effectiveness of the sFlt-1/PlGF ratio test globally for pregnant patients at-risk of developing PE.</div></div><div><h3>Data sources</h3><div>PubMed, Medline (OVID), National Health Service Economic Evaluation Database, Web of Science, Econlit, and Cost Effectiveness Analysis Registry was systematically searched between 2013-April 2023.</div></div><div><h3>Study eligibility criteria</h3><div>Empirical studies quantifying costs of the sFlt-1/PlGF ratio test compared to other diagnostic options for pregnant patients with suspected PE.</div></div><div><h3>Study appraisal and synthesis methods</h3><div>Eleven studies were included in the systematic review; all were cost analyses and modelled economic evaluations, and most used a health system perspective. Cost data were extracted into tables and indexed to 2022 United States Dollars (USD). An assessment of risk of bias for each study was performed using the Drummond critical appraisal checklist.</div></div><div><h3>Results</h3><div>All studies reported “cost-savings” of the test in antenatal care. Studies varied with costs and assumptions included, therefore a large range of incremental cost savings per patient was reported ($15–$1,881, 2022USD). No Incremental Cost-Effectiveness Ratios or health outcomes including Quality Adjusted Life Years were reported.</div></div><div><h3>Conclusions</h3><div>The included studies demonstrated “cost-savings” of the sFlt-1/PlGF ratio test in antenatal care for at-risk pregnant patients. 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引用次数: 0
摘要
目的先兆子痫(PE)影响约2%-4%的妊娠。诊断包括反复评估怀孕患者的危险因素。sFlt-1/PlGF比值试验在诊断和排除高危患者PE方面具有临床应用价值。通过排除PE的可能性,在产前保健中增加sFlt-1/PlGF比率测试可以防止不必要的住院、强化管理和早产,从而降低成本。本系统综述的目的是确定sFlt-1/PlGF比值测试在全球范围内对有PE风险的妊娠患者的成本效益。数据来源:pubmed, Medline (OVID), National Health Service Economic Evaluation Database, Web of Science, Econlit, Cost - Effectiveness Analysis Registry在2013年4月至2023年4月间系统检索。研究资格标准实证研究量化了sFlt-1/PlGF比值测试与其他诊断方案相比对疑似PE的妊娠患者的成本。研究评价与综合方法:系统评价纳入6项研究;所有这些都是成本分析和模拟经济评估,大多数是从卫生系统的角度进行的。成本数据被提取到表格中,并以2022年美元(USD)为索引。使用Drummond关键评价表对每项研究的偏倚风险进行评估。结果所有的研究都报告了产前检查的“成本节约”。研究因成本和假设的不同而有所不同,因此报告的每位患者的增量成本节约范围很大(15 - 1,881,2022美元)。未报告增量成本-效果比或包括质量调整生命年在内的健康结果。结论纳入的研究表明,sFlt-1/PlGF比值检测在高危孕妇产前护理中“节省了成本”。然而,这并没有考虑到健康结果的差异以及长期医疗保健的利用和支出。
Cost-effectiveness of the sFlt-1/PlGF ratio test in pregnant patients with suspected pre-eclampsia: a systematic review
Objectives
Pre-eclampsia (PE) affects approximately 2%–4% of pregnancies. Diagnosis involves repeated assessment of pregnant patients with risk factors. The sFlt-1/PlGF ratio test is shown to have clinical utility in ruling in and out PE among at-risk patients. By excluding the probability of PE, the addition of the sFlt-1/PlGF ratio test to antenatal care may prevent unnecessary hospital admissions, intensive management, and premature delivery, thus reducing costs. The objective of this systematic review is to determine the cost-effectiveness of the sFlt-1/PlGF ratio test globally for pregnant patients at-risk of developing PE.
Data sources
PubMed, Medline (OVID), National Health Service Economic Evaluation Database, Web of Science, Econlit, and Cost Effectiveness Analysis Registry was systematically searched between 2013-April 2023.
Study eligibility criteria
Empirical studies quantifying costs of the sFlt-1/PlGF ratio test compared to other diagnostic options for pregnant patients with suspected PE.
Study appraisal and synthesis methods
Eleven studies were included in the systematic review; all were cost analyses and modelled economic evaluations, and most used a health system perspective. Cost data were extracted into tables and indexed to 2022 United States Dollars (USD). An assessment of risk of bias for each study was performed using the Drummond critical appraisal checklist.
Results
All studies reported “cost-savings” of the test in antenatal care. Studies varied with costs and assumptions included, therefore a large range of incremental cost savings per patient was reported ($15–$1,881, 2022USD). No Incremental Cost-Effectiveness Ratios or health outcomes including Quality Adjusted Life Years were reported.
Conclusions
The included studies demonstrated “cost-savings” of the sFlt-1/PlGF ratio test in antenatal care for at-risk pregnant patients. However, this does not account for health outcome differences and long-term health care utilisation and expenditure.
AJOG global reportsEndocrinology, Diabetes and Metabolism, Obstetrics, Gynecology and Women's Health, Perinatology, Pediatrics and Child Health, Urology